"MEDCHEMEXPRESS"
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 100 MM IN DMSO；
FR180204 IS A POTENT AND SELECTIVE ATP-COMPETITIVE INHIBITOR OF ERK1 AND ERK2 WITH KI VALUE OF 0.31 UM AND 0.14 UM RESPECTIVELY HAS IC50 VALUES OF 0.51 AND 0.33 ΜM IN ENZYMATIC ASSA 1 * 1 mL
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 100 MM IN DMSO；
FR180204 IS A POTENT AND SELECTIVE ATP-COMPETITIVE INHIBITOR OF ERK1 AND ERK2 WITH KI VALUE OF 0.31 UM AND 0.14 UM RESPECTIVELY HAS IC50 VALUES OF 0.51 AND 0.33 ΜM IN ENZYMATIC ASSA 1 * 1 mL
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LIQUID FORMAT IS 10MM*1ML IN DMSO 1 * 10 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO 1 * 10 mg
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4-((2,6-DICHLOROPHENYL)THIO)-3-(5,6-DIMETHOXYISOINDOLINE-2-CARBONYL)-6-(TRIFLUOROMETHYL)PYRIDIN-2(1H)-ONE 1 * 100 mg
Supplier: MEDCHEMEXPRESS
4-((2,6-DICHLOROPHENYL)THIO)-3-(5,6-DIMETHOXYISOINDOLINE-2-CARBONYL)-6-(TRIFLUOROMETHYL)PYRIDIN-2(1H)-ONE 1 * 100 mg
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LIQUID FORMAT IS 10MM*1ML IN WATER
SOLUBILITY: H2O: 56MG/ML
OSELTAMIVIR ACID (GS 4071 RO 64-0802) IS A METABOLITE OF OSELTAMI VIR. OSELTAMIVIR IS A COMPETITIVE NEURAMINIDASE INHIBITOR, WHICH IS AN ANTIVIRAL DRUG. IC50 VALUE:TARGET: INFLUENZA V 1 * 50 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN WATER
SOLUBILITY: H2O: 56MG/ML
OSELTAMIVIR ACID (GS 4071 RO 64-0802) IS A METABOLITE OF OSELTAMI VIR. OSELTAMIVIR IS A COMPETITIVE NEURAMINIDASE INHIBITOR, WHICH IS AN ANTIVIRAL DRUG. IC50 VALUE:TARGET: INFLUENZA V 1 * 50 mg
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GLUCOCORTICOID RECEPTOR AGONIST-2 1 * 5 mg
Supplier: MEDCHEMEXPRESS
GLUCOCORTICOID RECEPTOR AGONIST-2 1 * 5 mg
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3-(difluoromethyl)-N-(6-((5S6S)-6-hydrox 1 * 10 mg
Supplier: MEDCHEMEXPRESS
3-(difluoromethyl)-N-(6-((5S6S)-6-hydrox 1 * 10 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO ≥70MG/ML WATER <1.2MG/ML ETHANOL <0.8MG/ML
TUBASTATIN A HCL IS A POTENT AND SELECTIVE HDAC6 INHIBITOR WITH IC50 OF 15 NM IS SELECTIVE (1000-FOLD MORE) AGAINST ALL OTHER ISOZYMES EXCEPT HDAC8 I 1 * 50 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO ≥70MG/ML WATER <1.2MG/ML ETHANOL <0.8MG/ML
TUBASTATIN A HCL IS A POTENT AND SELECTIVE HDAC6 INHIBITOR WITH IC50 OF 15 NM IS SELECTIVE (1000-FOLD MORE) AGAINST ALL OTHER ISOZYMES EXCEPT HDAC8 I 1 * 50 mg
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4-((14-amino-3.6.9.12-tetraoxatetradecyl)amino)-2-( 2.6-dioxo piperidin-3-yl)isoindoline-1.3-dione 1 * 100 mg
Supplier: MEDCHEMEXPRESS
4-((14-amino-3.6.9.12-tetraoxatetradecyl)amino)-2-( 2.6-dioxo piperidin-3-yl)isoindoline-1.3-dione 1 * 100 mg
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SOLUBILITY: DMSO:30MG/ML
RPR-260243 IS A NOVEL ACTIVATOR OF HERG MODIFIES HERG CURRENTS INHIBITED BY DOFETILIDE (IC50 = 58 NM) LITTLE EFFECT ON HERG CURRENT AMPLITUDE AND NO SIGNIFICANT EFFECTS ON STEADY-STATE ACTIVATION PARAMETERS OR ON CHANNEL 1 * 50 mg
Supplier: MEDCHEMEXPRESS
SOLUBILITY: DMSO:30MG/ML
RPR-260243 IS A NOVEL ACTIVATOR OF HERG MODIFIES HERG CURRENTS INHIBITED BY DOFETILIDE (IC50 = 58 NM) LITTLE EFFECT ON HERG CURRENT AMPLITUDE AND NO SIGNIFICANT EFFECTS ON STEADY-STATE ACTIVATION PARAMETERS OR ON CHANNEL 1 * 50 mg
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NUTLIN CARBOXYLIC ACID 1 * 25 mg
Supplier: MEDCHEMEXPRESS
NUTLIN CARBOXYLIC ACID 1 * 25 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO ≥90MG/ML WATER <1.2MG/ML ETHANOL ≥15MG/ML
ENZALUTAMIDE (MDV3100) IS AN ANDR OGEN-RECEPTOR (AR) ANTAGONIST WITH IC50 OF 36 NM.IC50 VALUE: 36 NM [1]TARGET: ANDROGEN-RECEPTORIN VITRO: ENZALUTAMIDE 1 * 500 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO ≥90MG/ML WATER <1.2MG/ML ETHANOL ≥15MG/ML
ENZALUTAMIDE (MDV3100) IS AN ANDR OGEN-RECEPTOR (AR) ANTAGONIST WITH IC50 OF 36 NM.IC50 VALUE: 36 NM [1]TARGET: ANDROGEN-RECEPTORIN VITRO: ENZALUTAMIDE 1 * 500 mg